NDC 51389-114 Take Cover Anti-aging Foundation Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51389 - Laura Geller Make Up Inc.
- 51389-114 - Take Cover Anti-aging Foundation
Product Packages
NDC Code 51389-114-03
Package Description: 29.57 g in 1 CONTAINER
Product Details
What is NDC 51389-114?
What are the uses for Take Cover Anti-aging Foundation Light?
Which are Take Cover Anti-aging Foundation Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Take Cover Anti-aging Foundation Light Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- TRIMETHYLOLPROPANE (UNII: 090GDF4HBD)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISODODECANE (UNII: A8289P68Y2)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- DIMETHICONOL (250000 MW) (UNII: RKI3S914RT)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CERAMIDE 2 (UNII: C04977SRJ5)
- PEG-10 RAPESEED STEROL (UNII: 258O76T85M)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LAURETH-12 (UNII: OAH19558U1)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- MICA (UNII: V8A1AW0880)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".